Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/25695
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dc.contributor.authorKılıç, İsmail-
dc.contributor.authorKilic, BA-
dc.contributor.authorGunay-Aygun, M-
dc.contributor.authorAksit, MA-
dc.date.accessioned2019-08-20T07:21:24Z-
dc.date.available2019-08-20T07:21:24Z-
dc.date.issued1997-
dc.identifier.issn0002-9297-
dc.identifier.urihttps://hdl.handle.net/11499/25695-
dc.description.abstractAbstract Not Availableen_US
dc.language.isoenen_US
dc.publisherUNIV CHICAGO PRESSen_US
dc.relation.ispartofAMERICAN JOURNAL OF HUMAN GENETICSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe association of ophthalmoplegia, severe myopia, and camptodactyly in two siblings of consanguineous parents. An autosomal recessive inherited entity?en_US
dc.typeConference Objecten_US
dc.identifier.volume61en_US
dc.identifier.issue4en_US
dc.identifier.issueSen_US
dc.identifier.startpageA103-
dc.identifier.startpageA103en_US
dc.identifier.endpageA103en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.identifier.wosWOS:000071446000580en_US
dc.ownerPamukkale_University-
item.openairetypeConference Object-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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